人民卫生出版社系列期刊
ISSN 2096-2738 CN 11-9370/R

中国科技核心期刊(中国科技论文统计源期刊)
2020《中国学术期刊影响因子年报》统计源期刊

新发传染病电子杂志 ›› 2018, Vol. 3 ›› Issue (3): 153-155.

• 论著 • 上一篇    下一篇

29例艾滋病相关淋巴瘤临床特点及预后因素分析

陈力, 刘敏, 何小庆, 吴玉珊, 李奇穗, 陈耀凯   

  1. 重庆市公共卫生医疗救治中心,重庆,400036
  • 收稿日期:2018-07-11 出版日期:2018-08-31 发布日期:2020-06-30
  • 通讯作者: 陈耀凯,Email:yoakiachen@hotmail.com
  • 基金资助:
    “十三五”国家科技重大专项(2018ZX10302104,2017ZX10202101-004-008)

Acquired Immunodeficiency Syndrome related lymphoma: 29 clinical cases and the factors influencing their prognosis

CHEN Li, LIU Min, HE Xiao-qing, WU Yu-shan, LI Qi-sui, CHEN Yao-kai   

  1. Chongqing Public Health Medical Center, Chongqing, 400000, China
  • Received:2018-07-11 Online:2018-08-31 Published:2020-06-30

摘要: 目的 分析艾滋病相关淋巴瘤(AIDS-related lymphoma,ARL)患者的临床特征,探讨其临床特征及影响预后的因素。方法 收集2015年1月至2017年12月由重庆市公共卫生医疗救治中心收治的29例ARL病例资料,按预后分为存活组和死亡组,回顾性分析其基础信息和临床症状。结果 29例患者的基线CD4细胞计数为(171.66±120.26)个/μl;临床表现:不明原因发热14例,淋巴结肿大10例,腹痛8例;病理特点:B细胞来源非霍奇金淋巴瘤(NHL)21例(72.41%),T细胞来源及霍奇金淋巴瘤(HL)8例(27.59%),IPI评分低危组4例(13.79%),中高危组25例(86.21%);共15例(51.72%)患者于就诊前及诊断淋巴瘤后1个月内接受HAART,按肿瘤科医师制定的方案规范化疗11例(37.93%);随访中死亡22例(75.86%),存活7例(24.14%)。单因素分析显示,预后影响因素包括IPI评分(OR=0.063,P<0.05)、是否接受规范化疗(OR=20.4,P<0.05)。结论 ARL主要为B细胞来源NHL,临床表现多样,就诊时多数已至淋巴瘤中晚期,病死率高,IPI评分及规范化学治疗是ARL患者预后的关键。

关键词: 获得性免疫缺陷综合征, 淋巴瘤, 化学治疗, 预后因素, 回顾性研究

Abstract: Objective To analyze 29 clinical cases of AIDS-related lymphoma (ARL) admitted to Chongqing Public Health Medical Center during the period from 2015 to 2017. Methods The clinical data of 29 patients with ARL admitted to Chongqing Public Health Medical Center were analyzed retrospectively for the clinical features and the factors influencing their prognosis. The subjects were divided into the survival group and the death group. Their basic data and clinical symptoms were analyzed. Results A total of 29 patients were recruited as the subjects of the study, including 22 were males and 7 females. The mean age was (50.76±14.58) years, and the baseline CD4 cell count was (171.66±120.26)/μL. Fourteen cases showed fever with no known reason, 10 cases lymphadenopathy and 8 cases abdominal pain. Based on the pathological findings, 21 cases(72.41%) were diagnosed with B cell non-Hodgkin's lymphoma (NHL), 8 cases(27.59%) with T cell origin and Hodgkin lymphoma (HL), 4 cases at IPI score-related middle-risk and 25 cases at high-risk (86.21%). In total,15 cases(51.72%) had received highly active antiretroviral therapy (HAART) before their first presentation to our hospital or within one month after the diagnosis of lymphoma. And 11 cases (37.93%) received standard chemotherapy regimen formulated by the oncology specialists. Twenty-two cases of death occurred, with a mortality rate of 75.86%. Univariate analysis showed that prognostic factors included IPI score (OR=0.063, P<0.05) and standard chemotherapy (OR=20.4, P<0.05). Conclusion ARL is mainly B cell-originated NHL and it has various clinical manifestations. Most of the patients are already in their intermediate or advanced stage of lymphoma and the mortality rate is high. IPI score and standard chemotherapy regimen are the key to the prognosis of patients with ARL.

Key words: Acquired immunodeficiency syndrome, Lymphoma, Chemotherapy, Prognostic factors, Retrospective studies